Variant · Snv
HNF4A NM_175914.5(HNF4A):c.999C>G (p.Ile333Met)
CI-VAR-00362927Explore in graph →p.Ile333MetNM_175914.5:c.999C>GClinVar 3587260
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 3587260 | Likely benign | reviewed by expert panel | 3 | Type 2 diabetes mellitus; Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young; Maturity-onset diabetes of the young type 1; Monogenic diabetes | germline | 3 | Jul 16, 2025 | clinvar |